A rare cause for primary amenorrhea: Sporadic perrault syndrome

A rare cause for primary amenorrhea: Sporadic perrault syndrome

Gonadal (ovarian) dysgenesis with normal chromosomes (46, XX), XX female gonadal dysgenesis (XX-GD) is a rare genetically heterogeneous disorder. In 1951, Perrault reported the association of gonadal dysgenesis and deafness, now referred to as Perrault syndrome. Perrault syndrome is a rare autosomal...

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Bibliographic Details
Main Authors: K H Noorul Ameen, Rakesh Pinninti
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2012-01-01
Series:Indian Journal of Endocrinology and Metabolism
Subjects:
Deafness
karyotype
marfanoid habitus
ovarian dysgenesis
Perrault syndrome
Online Access:http://www.ijem.in/article.asp?issn=2230-8210;year=2012;volume=16;issue=5;spage=843;epage=845;aulast=Noorul

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http://www.ijem.in/article.asp?issn=2230-8210;year=2012;volume=16;issue=5;spage=843;epage=845;aulast=Noorul

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